Question 1: What suffix is used in the names of esters?
a) -ol
b) -al
c) -ate
d) -one
Question 2: What catalyst is necessary for the esterification reaction to take place?
a) H2SO4
b) H2CO3
c) HCI
d) HNO3
1)suffix is used in the names of esters is -oate.
2)Esters are produced when carboxylic acids are heated with alcohols in the presence of an acid catalyst. The catalyst is usually concentrated sulphuric acid. So (a) is the correct option.
Question 1: What suffix is used in the names of esters? a) -ol b) -al c)...
Name Experiment 7 - PREPARATION OF ASPIRIN AND OTHER ESTERS Date Partner Station # - Pre-Lab Preparation Section Questions 1-3 refer to these structures: CH,CH-O-CH,CH, CH,CH,CH,CH.CH.CH-OH CH,-0-0-CH,CH.CH, O anch-o- & -on,ch, and on and ansch.com 1. a) List the letters for the structures that are esters. b) Circle the ester functional group in any esters. 2. a) Write the letters for the two compounds that could be used to make an ester by an esterification reaction. b) Write the reaction...
A: Esterification ive: To make three common esters and to note their characteristic odour and to draw structural diagrams representing each reactions. Set up a 400 mL beaker and apparatus like the example on the front lab bench. Fill the beaker approximately 2/3 full of water to serve as a hot bath. For each of the carboxylic acid- alcohol pair of chemicals below, complete the following Note that the carboxylic acid may be a crystal or a solution. 1. Carefully...
1 a) For each of the following compounds, give the IUPAC suffix and the chain length as demonstrated for the example. Compound IUPAC Chain Compound IUPAC Chain suffix length suffix length OH -ol 4 OH alcohol OH O w nii CHE Br i Ulo OH N(CH3)2 b) Match each of the following structures with the proper IUPAC name. Note that there are more names than structures (not all names will be used). CH3 Br CI Br Br CH, a) 2,4-dimethyl-1,3-cyclopentadiene...
CH, Bre, light CI 1 Brz, AIBr; A B AICI HNO, c CO, HCI; Cuci, AICI3 H2SO4 D CH3 HNO3, H2SO4 H F Br SO; H2SO4 G E CO2 I со, A= B= C= D= E= F= G= H= Which reaction sequence best accomplishes this transformation: NO2 SOZH OCH3 Br OCHZ You a) SO3 H2SO4 Pd(OAC)2 HNO, H2SO4 AICI (HO)2B OCH b) HNO3 H2SO4 SO3 H2SO4 Br2 AICI: Pd(OAc)2, base (HO),B. OCH3 c) Zn(Hg) HCI, H20 HNO3 H2SO4 SO, H2SO4...
Question 4 Waxes are high molar mass: A)Fatty acids B) Esters C)Alcohols D) Amides B Question 5 Provide the reagent(s) necessary to carry out the following conversion. COCHE OH A) 1) one equivalent CH3MgBr/ether 2) H2O B) excess CH3MgBr/ether/H2O C) 1) excess CH3MgBr/ether 2) H2O D) all the above A В C Question 6 Which one is not a complex lipid? AyWaxes B) steroids Phospholipids D) Triglycerides A B С D
CHE2613/101/3/2020 2. Provide the IUPAC names of the reactants and product expected from each of the reactions below. (Where there is no reaction provide reasons) a) CH2CH3 Bry/FeBrg b) CH3 HNO3/H2SO4 OCH3 OCH3 SOZ/H2SO4 NO2 d) CH2CH3 (CH3)3CCI/AICI: . Attempted conversion of aniline to p-aminoacetophenone using acetal chloride and aluminum chloride fails even when an excess of the catalyst is used. Explain this observation in detail. 23
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6. What is the major product of the following reaction? Br AL с NOZ NO, B NO 7. At which site on the following substrate will electrophilic substitution be most likely to occur, in the formation of a mono-substituted product? N(CH3)2 Br 8. Select the reagents and the appropriate sequence to prepare the product shown below from benzene, with the best possible yield. NO a) (1) HNO3, H2SO4, [2] MeCOCI, AICI: b) [1] MeCOCI, AICI, [2] HNO3,...
Question 1 What is the major organic product of the following reaction sequence? Type its systematic IUPAC name in the box below. 1) HNO3, H2SO4 2) Sn, HCI 3) NaNO2, HCI, O°C 4) CuCN 5) H2SO4, H20, heat
8. What is the major product formed from the reaction shown? 1. CHẠI 2. Ag,0,H, A. III B. 1 C. II D. IV E. II and III F. I and IV 9. Select the reaction sequence that will produce the desired product HNO3, H2SO 1.Sn.HCI NANO,.HCI Cur 2.NaOH HNO, H SO. 1.Sn, HCI CuBr PCC 2.NaOH HNO3, H2SO 1.Sn, HCI NANO.HCI Bre, FeBr3 2.NaOH HNO3, H2SO4 Bry, FeBr 1.Sn, HCI 1.NaNO2.HCI 2.NaOH 2. H,O, heat HNO3, H2SO4 1.Sn, HCI NaNO,,HCI...
Organic chemistry lab performing small scale Fisher esterification to make a variety of esters. 1) If you were doing these experiments on a larger scale, describe two ways that you could improve the yield of the target ester. 2) What is the point of adding sulfuric acid to the reaction? How about the heat? 3) Write the mechanism for the formation of wintergreen with 0.20g of anthranilic acid, 6 drops of methanol and one drop of H2SO4, then heated for...